Medical device developers and diagnostics companies are faced with a range of unique challenges – from navigating sometimes vague regulatory guidelines to planning complex clinical trials to staying on top of recent deal activities and competitor product advancements. As one of the most complex and high-tech industries, implementing cost-effective business development, clinical and regulatory strategies is imperative to efficiently make strategic decisions, keep track of key development milestones and navigate your way to launch.
Get the help you need from the Cortellis™ suite of life science intelligence solutions. We curate the broadest and deepest sources of intelligence to enable precise, actionable answers to your specific questions across the device development lifecycle – from clinical development and regulatory strategy through commercialization and launch.
Bring speed and certainty across the development lifecycle
Maintain your competitive edge.
Focus your research and maximize your chances of success.
Have greater confidence in your regulatory strategies.
With the ever-changing regulatory landscape, it’s easy to miss a critical piece of information that can throw off your strategy. Navigate the regulatory landscape and make more informed decisions with insights from Cortellis.
Access exclusive deals intelligence that covers all types of partnerships and get a comprehensive foundation for analysis and decision-making with Cortellis Digital Health Intelligence™.
Regulatory authorities
Regulatory documents
Original articles researched and written by our news staff every year
Device deals over 20 years
Broker research reports
Diseases and surgical procedures
Our accredited global alliance program delivers value-added solutions by combining offerings from Clarivate with other technology and service providers. Partner with us to drive profitable growth, increase revenue and deliver greater value to your customers.
Contact us to learn more about how we serve medical device companies.